HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → (S)-1-Boc-3-methylpiperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (R)-1-Boc-2-tert-butyl-3-methyl-4-imidazolidinone | HCID 546472 | — |
| Reactant | 2-Methylpiperazine, (S)- | HCID 2734219 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | (S)-1-Boc-3-methylpiperazine | HCID 7023035 | — |
Reaction Steps
To a solution of 1-(tert-butoxycarbonyl)-2-tert-butyl-3-methyl-4-imidazolidinone (2 g, 8,3 mmol) (BOC-ON) in chloroform (15 ml) was added (2S)-2-methylpiperazine (5 g, 50 mmol), a compound of formula (6), and triethylamine (1.25 g, 12.5 mmol) in chloroform. The mixture was stirred for about 15 hours at room temperature, and then washed with water, the solvent removed from the organic layer under reduced pressure, and the residue purified using column chromatography, to give tert-butyl (3S)-3-methylpiperazinecarboxylate, a compound of formula (7).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07125876B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-78406fa2b2bf40b592a8bd1e26a9c340 |
| Source note | uspto-grants-2006_10 |